Reidemeister S - Search Results

1

1-Alkyl-4-phenyl-6-alkoxy-1H-quinazolin-2-ones: a novel series of potent calcium-sensing receptor antagonists.

Widler L, Altmann E, Beerli R, Breitenstein W, Bouhelal R, Buhl T, Gamse R, Gerspacher M, Halleux C, John MR, Lehmann H, Kalb O, Kneissel M, Missbach M, Müller IR, Reidemeister S, Renaud J, Taillardat A, Tommasi R, Weiler S, Wolf RM, Seuwen K. Widler L, et al. Among authors: reidemeister s. J Med Chem. 2010 Mar 11;53(5):2250-63. doi: 10.1021/jm901811v. J Med Chem. 2010. PMID: 20158186

2

Development of chiral N-alkylcarbamates as new leads for potent and selective H3-receptor antagonists: synthesis, capillary electrophoresis, and in vitro and oral in vivo activity.

Sasse A, Kiec-Kononowicz K, Stark H, Motyl M, Reidemeister S, Ganellin CR, Ligneau X, Schwartz JC, Schunack W. Sasse A, et al. Among authors: reidemeister s. J Med Chem. 1999 Feb 25;42(4):593-600. doi: 10.1021/jm9804376. J Med Chem. 1999. PMID: 10052966

3

Novel partial agonists for the histamine H(3) receptor with high in vitro and in vivo activity.

Sasse A, Stark H, Reidemeister S, Hüls A, Elz S, Ligneau X, Ganellin CR, Schwartz JC, Schunack W. Sasse A, et al. Among authors: reidemeister s. J Med Chem. 1999 Oct 7;42(20):4269-74. doi: 10.1021/jm991068w. J Med Chem. 1999. PMID: 10514298

4

Novel histamine H3 receptor antagonists: affinities in an H3 receptor binding assay and potencies in two functional H3 receptor models.

Schlicker E, Kathmann M, Reidemeister S, Stark H, Schunack W. Schlicker E, et al. Among authors: reidemeister s. Br J Pharmacol. 1994 Aug;112(4):1043-8. doi: 10.1111/j.1476-5381.1994.tb13188.x. Br J Pharmacol. 1994. PMID: 7952862 Free PMC article.

5

Novel histamine H3-receptor antagonists with benzyl ether structure or related moieties: synthesis and structure-activity relationships.

Hüls A, Purand K, Stark H, Reidemeister S, Ligneau X, Arrang JM, Schwartz JC, Schunack W. Hüls A, et al. Among authors: reidemeister s. Arch Pharm (Weinheim). 1996 Aug-Sep;329(8-9):379-85. doi: 10.1002/ardp.19963290802. Arch Pharm (Weinheim). 1996. PMID: 8915097

6

Substituted N-phenylcarbamates as histamine H3 receptor antagonists with improved in vivo potency.

Reidemeister S, Stark H, Ligneau X, Ganellin CR, Schwartz JC, Schunack W. Reidemeister S, et al. Pharmazie. 2000 Feb;55(2):83-6. Pharmazie. 2000. PMID: 10723763

7

(Partial) agonist/antagonist properties of novel diarylalkyl carbamates on histamine H3 receptors.

Sasse A, Stark H, Ligneau X, Elz S, Reidemeister S, Ganellin CR, Schwartz JC, Schunack W. Sasse A, et al. Among authors: reidemeister s. Bioorg Med Chem. 2000 May;8(5):1139-49. doi: 10.1016/s0968-0896(00)00050-x. Bioorg Med Chem. 2000. PMID: 10882024

8

Potencies of antagonists chemically related to iodoproxyfan at histamine H3 receptors in mouse brain cortex and guinea-pig ileum: evidence for H3 receptor heterogeneity?

Schlicker E, Kathmann M, Bitschnau H, Marr I, Reidemeister S, Stark H, Schunack W. Schlicker E, et al. Among authors: reidemeister s. Naunyn Schmiedebergs Arch Pharmacol. 1996 Apr;353(5):482-8. doi: 10.1007/BF00169166. Naunyn Schmiedebergs Arch Pharmacol. 1996. PMID: 8740140

9

A Composite Endpoint for Acceptability Evaluation of Oral Drug Formulations in the Pediatric Population.

Wargenau M, Reidemeister S, Klingmann I, Klingmann V. Wargenau M, et al. Among authors: reidemeister s. Ther Innov Regul Sci. 2022 Nov;56(6):903-909. doi: 10.1007/s43441-022-00406-z. Epub 2022 Apr 26. Ther Innov Regul Sci. 2022. PMID: 35471561 Free PMC article.

10

Validating a composite endpoint for acceptability evaluation of oral drug formulations in the pediatric population: a randomized, open-label, single dose, cross-over study.

Münch J, Schwarzwälder AL, Kloft C, Bosse HM, Wargenau M, Reidemeister S, Klingmann I, Klingmann V. Münch J, et al. Among authors: reidemeister s. Front Pharmacol. 2024 Aug 19;15:1436554. doi: 10.3389/fphar.2024.1436554. eCollection 2024. Front Pharmacol. 2024. PMID: 39224774 Free PMC article.

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